Newborn Screening Panel

This product is only meant for customers who already purchased a Dante Genome Test

Newborn Screening Panel is a routine screening test that is performed shortly after birth to identify genetic disorders that can cause serious health problems if not detected and treated early. The panel tests for a wide range of genetic disorders, including metabolic disorders, endocrine disorders, and hemoglobinopathies, among others.
This panel is recommended for all newborns, as early detection and treatment can prevent or reduce the severity of many genetic disorders. Testing can provide valuable information to healthcare providers and parents, such as identifying infants who may need further testing or treatment. It can also provide reassurance for parents of unaffected infants.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • More than 1040 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Phenylketonuria
  • Congenital hypothyroidism
  • Galactosemia
  • Sickle cell disease
  • Cystic fibrosis
  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Maple syrup urine disease
  • Homocystinuria
  • Biotinidase deficiency

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